Lisa E Kratz
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Explore the profile of Lisa E Kratz including associated specialties, affiliations and a list of published articles.
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22
Citations
430
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Recent Articles
1.
Tierney E, Remaley A, Thurm A, Jager L, Wassif C, Kratz L, et al.
Transl Psychiatry
. 2021 Sep;
11(1):471.
PMID: 34504056
An improved understanding of sterol and lipid abnormalities in individuals with autism spectrum disorder (ASD) could lead to personalized treatment approaches. Toward this end, in blood, we identified reduced synthesis...
2.
Maceda E, Kratz L, Ramos V, Abacan M
BMJ Case Rep
. 2020 Nov;
13(11).
PMID: 33139364
We report a case of a 1-year and 2-month-old girl with clinical features consistent with congenital hemidysplasia with ichthyosis and limb defects syndrome. Sterol analysis from skin flakes revealed increased...
3.
Collins M, Miranda V, Rousseau J, Kratz L, Campeau P
Bone
. 2020 Aug;
141:115601.
PMID: 32827848
Lamin B receptor, a member of the sterol reductase family, is an inner nuclear membrane protein which binds lamin B proteins and is involved in the organization of heterochromatin. Mutations...
4.
Knezevic C, Ness M, Kratz L, Marzinke M
Clin Chim Acta
. 2018 Jul;
486:94-97.
PMID: 30040921
Background: Intravenous immunoglobulin (IVIG) is prepared from the plasma of hundreds of blood donors and is used in the treatment of immunodeficiencies, autoimmune conditions, infections and inflammatory conditions. IVIG formulations...
5.
6.
Edmunds L, Otero P, Sharma L, DSouza S, Dolezal J, David S, et al.
Oncotarget
. 2016 Apr;
7(21):30379-95.
PMID: 27105497
Establishing c-Myc's (Myc) role in liver regeneration has proven difficult particularly since the traditional model of partial hepatectomy may provoke an insufficiently demanding proliferative stress. We used a model of...
7.
Driver A, Kratz L, Kelley R, Stottmann R
Neurobiol Dis
. 2016 Feb;
91:69-82.
PMID: 26921468
We previously reported a mutation in the cholesterol biosynthesis gene, hydroxysteroid (17-beta) dehydrogenase 7 (Hsd17b7(rudolph)), that results in striking embryonic forebrain dysgenesis. Here we describe abnormal patterns of neuroprogenitor proliferation...
8.
Gabitova L, Restifo D, Gorin A, Manocha K, Handorf E, Yang D, et al.
Cell Rep
. 2015 Sep;
12(11):1927-38.
PMID: 26344763
Meiosis-activating sterols (MAS) are substrates of SC4MOL and NSDHL in the cholesterol pathway and are important for normal organismal development. Oncogenic transformation by epidermal growth factor receptor (EGFR) or RAS...
9.
Dias C, Rupps R, Millar B, Choi K, Marra M, Demos M, et al.
Orphanet J Rare Dis
. 2014 Jun;
9:94.
PMID: 24961299
Desmosterolosis is an autosomal recessive disorder of cholesterol biosynthesis caused by biallelic mutations of DHCR24 (homozygous or compound heterozygous), which encodes 3-β-hydroxysterol Δ-24-reductase. We report two sisters homozygous for the...
10.
Sukhanova A, Gorin A, Serebriiskii I, Gabitova L, Zheng H, Restifo D, et al.
Cancer Discov
. 2012 Nov;
3(1):96-111.
PMID: 23125191
Unlabelled: Persistent signaling by the oncogenic EGF receptor (EGFR) is a major source of cancer resistance to EGFR targeting. We established that inactivation of 2 sterol biosynthesis pathway genes, SC4MOL...